Humatrope And Human Enhancement: Lilly Drug Featured In Bioethics Report
FDA's approval of Humatrope for idiopathic short stature plays a prominent role in a report by the President's Council on Bioethics as an example of the blurry line between medical need and human enhancement
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The Biotechnology Industry Organization is continuing to expand its reach into the health policy arena with the creation of a "chief of policy" position
An assessment of the long-term safety and efficacy of Lilly's Humatrope for idiopathic short stature will rely on a voluntary ongoing postmarket research program
Lilly should develop prescribing criteria to guide the use of Humatrope for non-growth hormone deficient short stature in pediatric patients, members of FDA's Endocrinologic & Metabolic Drugs Advisory Committee suggested during a June 10 meeting